We have previously described ProxiMAX, a technology that enables the fabrication of precise, combinatorial gene libraries via codon-by-codon saturation mutagenesis. ProxiMAX was originally performed using manual, enzymatic transfer of codons via blunt-end ligation. Here we present Colibra™: an automated, proprietary version of ProxiMAX used specifically for antibody library generation, in which double-codon hexamers are transferred during the saturation cycling process. The reduction in process complexity, resulting library quality and an unprecedented saturation of up to 24 contiguous codons are described. Utility of the method is demonstrated via fabrication of complementarity determining regions (CDR) in antibody fragment libraries and n...
The overall objective of this PhD project was to develop and validate methods for advancing the appl...
This article describes the generation of the Human Combinatorial Antibody Library HuCAL GOLD. HuCAL ...
textThis dissertation describes several strategies used to create diversity in non-immune antibody l...
We have previously described ProxiMAX, a technology that enables the fabrication of precise, combina...
We have previously described ProxiMAX, a technology that enables the fabrication of precise, combina...
Back in 2003, we published ‘MAX’ randomisation, a process of non-degenerate saturation mutagenesis u...
Back in 2003, we published ‘MAX ’ randomization, a process of non-degenerate saturation mutagenesis ...
Saturation mutagenesis is a powerful tool in modern protein engineering, which permits key residues ...
Phage display technology utilises peptide and antibody libraries with very high diversities to selec...
Antibody discovery by phage display consists of two phases, i.e., the binding phase and the amplific...
<div><p>Phage display technology has been widely used for antibody affinity maturation for decades. ...
Phage display technology has been widely used for antibody affinity maturation for de-cades. The lim...
We constructed a single-chain Fv antibody library that permits human complementarity-determining reg...
Saturation mutagenesis probes define sections of the vast protein sequence space. However, even if r...
In Nature, antibodies are capable of recognizing a huge variety of different molecular structures on...
The overall objective of this PhD project was to develop and validate methods for advancing the appl...
This article describes the generation of the Human Combinatorial Antibody Library HuCAL GOLD. HuCAL ...
textThis dissertation describes several strategies used to create diversity in non-immune antibody l...
We have previously described ProxiMAX, a technology that enables the fabrication of precise, combina...
We have previously described ProxiMAX, a technology that enables the fabrication of precise, combina...
Back in 2003, we published ‘MAX’ randomisation, a process of non-degenerate saturation mutagenesis u...
Back in 2003, we published ‘MAX ’ randomization, a process of non-degenerate saturation mutagenesis ...
Saturation mutagenesis is a powerful tool in modern protein engineering, which permits key residues ...
Phage display technology utilises peptide and antibody libraries with very high diversities to selec...
Antibody discovery by phage display consists of two phases, i.e., the binding phase and the amplific...
<div><p>Phage display technology has been widely used for antibody affinity maturation for decades. ...
Phage display technology has been widely used for antibody affinity maturation for de-cades. The lim...
We constructed a single-chain Fv antibody library that permits human complementarity-determining reg...
Saturation mutagenesis probes define sections of the vast protein sequence space. However, even if r...
In Nature, antibodies are capable of recognizing a huge variety of different molecular structures on...
The overall objective of this PhD project was to develop and validate methods for advancing the appl...
This article describes the generation of the Human Combinatorial Antibody Library HuCAL GOLD. HuCAL ...
textThis dissertation describes several strategies used to create diversity in non-immune antibody l...